PMID- 20674972 OWN - NLM STAT- MEDLINE DCOM- 20101220 LR - 20211020 IS - 1532-3102 (Electronic) IS - 0143-4004 (Print) IS - 0143-4004 (Linking) VI - 31 IP - 9 DP - 2010 Sep TI - Expression of regulatory T cell (Treg) activation markers in endometrial tissues from early and late pregnancy in the feline immunodeficiency virus (FIV)-infected cat. PG - 796-802 LID - 10.1016/j.placenta.2010.06.019 [doi] AB - Regulatory T cells (Tregs) support pregnancy maintenance by suppressing placental inflammation, while diminished Treg function may accompany reproductive failure. Experimental FIV infection frequently results in vertical transmission and increased pregnancy failure in the cat. The mechanism of reproductive compromise is unknown. We hypothesized that FIV infection alters endometrial Treg population dynamics and function, potentiating vertical transmission and reproductive failure. RNA collected from early and late gestation reproductive tissue and fetuses from FIV infected and control cats was probed for expression of FIV gag and Treg markers CD25, FOXP3, and CTLA4, using real time reverse-transcriptase (RT)-PCR. Frequent placental and fetal infection and reproductive failure were detected at early and late pregnancy. Expression of FOXP3 and CTLA4 was higher in early gestation tissues from control cats. FIV infection significantly reduced expression of FOXP3 and CTLA4 at early, but not late pregnancy. At late pregnancy, CTLA4 was expressed to higher levels in infected tissues. The number of tissues with decreased co-expression of FOXP3 and CTLA4 was significant in infected cats at early pregnancy. No significant changes in CD25 expression occurred between FIV-infected and control animals at early or late pregnancy. Differences in Treg marker expression were not significant between viable and non-viable pregnancies in infected cats. The detection of Treg markers in these feline tissues provides the first evidence of feline endometrial Tregs and suggests that such cells diminish as pregnancy progresses. These cells may be depleted or rendered less functional by viral infection, but understanding their role in pregnancy requires further study. CI - Published by Elsevier Ltd. FAU - Lockett, N N AU - Lockett NN AD - Department of Biological Sciences, Mississippi State University, Mississippi State, MS 39762, USA. FAU - Scott, V L AU - Scott VL FAU - Boudreaux, C E AU - Boudreaux CE FAU - Clay, B T AU - Clay BT FAU - Pruett, S B AU - Pruett SB FAU - Ryan, P L AU - Ryan PL FAU - Coats, K S AU - Coats KS LA - eng GR - R15 AI048419/AI/NIAID NIH HHS/United States GR - R15 AI048419-02A1/AI/NIAID NIH HHS/United States GR - 2R15AI048419-02A1/AI/NIAID NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural DEP - 20100802 PL - Netherlands TA - Placenta JT - Placenta JID - 8006349 RN - 0 (Antigens, CD) RN - 0 (CTLA-4 Antigen) RN - 0 (Forkhead Transcription Factors) RN - 0 (Interleukin-2 Receptor alpha Subunit) SB - IM MH - Animals MH - Antigens, CD/biosynthesis MH - CTLA-4 Antigen MH - Cats MH - Feline Acquired Immunodeficiency Syndrome/*immunology MH - Female MH - Forkhead Transcription Factors/biosynthesis MH - Infectious Disease Transmission, Vertical/veterinary MH - Interleukin-2 Receptor alpha Subunit/biosynthesis MH - Pregnancy/immunology MH - Pregnancy Complications, Infectious/*veterinary MH - T-Lymphocytes, Regulatory/*immunology PMC - PMC2933968 MID - NIHMS223692 EDAT- 2010/08/03 06:00 MHDA- 2010/12/21 06:00 PMCR- 2011/09/01 CRDT- 2010/08/03 06:00 PHST- 2010/05/18 00:00 [received] PHST- 2010/06/25 00:00 [revised] PHST- 2010/06/29 00:00 [accepted] PHST- 2010/08/03 06:00 [entrez] PHST- 2010/08/03 06:00 [pubmed] PHST- 2010/12/21 06:00 [medline] PHST- 2011/09/01 00:00 [pmc-release] AID - S0143-4004(10)00249-3 [pii] AID - 10.1016/j.placenta.2010.06.019 [doi] PST - ppublish SO - Placenta. 2010 Sep;31(9):796-802. doi: 10.1016/j.placenta.2010.06.019. Epub 2010 Aug 2.